BOVILIS RINGVAC Hrvatska - hrvatski - Ministarstvo poljoprivrede, Uprava za Veterinarstvo i sigurnost hrane

bovilis ringvac

intervet international b.v., podružnica u republici hrvatskoj, ivana lučića 2a, 10000 zagreb, hrvatska - mikrokonidije nevirulentnog soja ltf-130 trichophyton verrucosum - liofilizat i otapalo za suspenziju za injekciju - imunološki vmp - goveda

Xaluprine (previously Mercaptopurine Nova Laboratories) Europska Unija - hrvatski - EMA (European Medicines Agency)

xaluprine (previously mercaptopurine nova laboratories)

nova laboratories ireland limited - 6-merkaptopurin monohidrat - leukemija, limfoid - antineoplastična sredstva - xaluprin je indiciran za liječenje akutne limfoblastične leukemije (all) u odraslih, adolescenata i djece.

Dimenium 50 mikrograma + 100 mikrograma u jednoj dozi, prašak inhalata, dozirani Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

dimenium 50 mikrograma + 100 mikrograma u jednoj dozi, prašak inhalata, dozirani

elpen pharmaceutical co.inc. (sa), 95, marathonos ave., pikermi, attica, grčka - salmeterolksinafoat flutikazonpropionat - prašak inhalata, dozirani - 50 mikrograma + 100 mikrograma - urbroj: jedna doza praška inhalata sadrži 50 mikrograma salmeterola u obliku salmeterolksinafoata i 100 mikrograma flutikazonpropionata

Dimenium 50 mikrograma + 250 mikrograma u jednoj dozi, prašak inhalata, dozirani Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

dimenium 50 mikrograma + 250 mikrograma u jednoj dozi, prašak inhalata, dozirani

elpen pharmaceutical co.inc. (sa), 95, marathonos ave., pikermi, attica, grčka - salmeterolksinafoat flutikazonpropionat - prašak inhalata, dozirani - 50 mikrograma + 250 mikrograma - urbroj: jedna doza praška inhalata sadrži 50 mikrograma salmeterola u obliku salmeterolksinafoata i 250 mikrograma flutikazonpropionata

Dimenium 50 mikrograma + 500 mikrograma u jednoj dozi, prašak inhalata, dozirani Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

dimenium 50 mikrograma + 500 mikrograma u jednoj dozi, prašak inhalata, dozirani

elpen pharmaceutical co.inc. (sa), 95, marathonos ave., pikermi, attica, grčka - salmeterolksinafoat flutikazonpropionat - prašak inhalata, dozirani - 50 mikrograma + 500 mikrograma - urbroj: jedna doza praška inhalata sadrži 50 mikrograma salmeterola u obliku salmeterolksinafoata i 500 mikrograma flutikazonpropionata

Loxicom Europska Unija - hrvatski - EMA (European Medicines Agency)

loxicom

norbrook laboratories (ireland) limited - mcloksikam - anti-inflammatory and anti-rheumatic products, non-steroids - dogs; cats; cattle; pigs - dogsalleviation upale i bolova u akutni i kronični mišićno-koštanog sustava. smanjiti postoperativnu bol i upalu nakon operacije ortopedskih i mekih tkiva. catsalleviation upale i bolova u kroničnim poremećajima lokomotornog aparata kod mačaka. da bi se smanjila sobu za intenzivnu njegu bol nakon овариогистерэктомии i male mekih tkiva kirurgija. cattlefor koristiti i kod akutne infekcije respiratornog odgovarajuće antibiotske terapije za smanjenje kliničkih znakova u goveda. za upotrebu u proljevu u kombinaciji s oralnom rehidracijskom terapijom kako bi se smanjili klinički znakovi u teladi starijoj od jednog tjedna i mlade, ne-laktirajuće stoke. za pomoćnu terapiju u liječenju akutnog mastitisa, u kombinaciji s antibiotskom terapijom. koristiti pigsfor u неинфекционной bolestima mišićno-koštanog sustava za ublažavanje simptoma hromost i upale. za pomoćnu terapiju u liječenju puerperalne septikemije i toksemije (mastitis-metritis-agalaktia sindrom) s odgovarajućom terapijom antibioticima. horsesfor koristiti za smanjenje upale i ublažavanje boli u akutni i kronični mišićno-koštanog sustava. za olakšanje boli povezane s kolikom kolica.

Xromi Europska Unija - hrvatski - EMA (European Medicines Agency)

xromi

nova laboratories ireland limited - hidroksikarbamid - anemija, sickle cell - antineoplastična sredstva - prevencija сосудисто-jamice komplikacija anemija srpastih stanica anemije u bolesnika starijih od 2 godine.

Jayempi Europska Unija - hrvatski - EMA (European Medicines Agency)

jayempi

nova laboratories ireland limited - azathioprine - odbacivanje transplantata - imunosupresivi - jayempi is indicated in combination with other immunosuppressive agents for the prophylaxis of transplant rejection in patients receiving allogenic kidney, liver, heart, lung or pancreas transplants. azathioprine is indicated in immunosuppressive regimens as an adjunct to immunosuppressive agents that form the mainstay of treatment (basis immunosuppression). jayempi is used as an immunosuppressant antimetabolite either alone or, more commonly, in combination with other agents (usually corticosteroids) and/ or procedures which influence the immune response. jayempi is indicated in patients who are intolerant to glucocorticosteroids or if the therapeutic response is inadequate despite treatment with high doses of glucocorticosteroids, in the following diseases:severe active rheumatoid arthritis (chronic polyarthritis) that cannot be kept under control by less toxic agents (disease-modifying anti-rheumatic -medicinal products – dmards)auto-immune hepatitis systemic lupus erythematosusdermatomyositispolyarteritis nodosapemphigus vulgaris and bullous pemphigoidbehçet’s diseaserefractory auto-immune haemolytic anaemia, caused by warm igg antibodieschronic refractory idiopathic thrombocytopenic purpurajayempi is used for the treatment of moderately severe to severe forms of chronic inflammatory bowel disease (ibd) (crohn’s disease or ulcerative colitis) in patients in whom glucocorticosteroid therapy is necessary, but where glucocorticosteroids are not tolerated, or in whom the disease is untreatable with other common means of first choice. it is also indicated in adult patients in relapsing multiple sclerosis, if an immunomodulatory therapy is indicated but beta interferon therapy is not possible, or a stable course has been achieved with previous treatment with azathioprine. 3jayempi is indicated for the treatment of generalised myasthenia gravis. depending on the severity of the disease, jayempi should be given in combination with glucocorticosteroids because of slow onset of action at the beginning of treatment and the glucocorticosteroid dose should be gradually reduced after several months of treatment.

Qaialdo Europska Unija - hrvatski - EMA (European Medicines Agency)

qaialdo

nova laboratories ireland limited - spironolakton - edema; heart failure; liver cirrhosis; ascites; nephrotic syndrome; hyperaldosteronism; essential hypertension - antihypertensives and diuretics in combination - in the management of refractory oedema associated with congestive cardiac failure; hepatic cirrhosis with ascites and oedema, malignant ascites, nephrotic syndrome, diagnosis and treatment of primary aldosteronism, essential hypertension. neonates, children and adolescents should only be treated under guidance of a paediatric specialist (see sections 5. 1 i 5.